Novel salts and crystals

ABSTRACT

The disclosure provides a new, stable, pharmaceutically acceptable bis-tosylate salt form of 1-(4-fluoro-phenyl)-4-((6bR, 10aS)-3-methyl-2,3,6b,9, 10, 10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxalin-8-yl)-butan-1-one, together with methods of making and using them, and pharmaceutical compositions comprising them.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is an International Application which claims benefit to and priority from U.S. Provisional Application No. 62/681,534, filed on Jun. 6, 2018, the contents of which are hereby incorporated by reference in its entirety.

FIELD

This disclosure relates to certain salts and crystal forms of a substituted heterocycle fused gamma-carboline, the manufacture thereof, pharmaceutical compositions thereof, and use thereof, e.g., in the treatment of diseases or abnormal conditions involving or mediated by the 5-HT_(2A) receptor, serotonin transporter (SERT), and/or dopamine D₁/D₂ receptor signaling pathways.

BACKGROUND

1-(4-fluorophenyl)-4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxalin-8-yl)-butan-1-one (sometimes referred to as 4-((6bR,10aS)-3 -methyl-2,3,6b,9,10, 10a-hexahydro-1H-pyrido[3′,4′:4,5]pyrrolo[1,2,3 -de]quinoxalin-8(7H)-yl)-1-(4-fluorophenyl)-1-butanone, and also known as Lumateperone or as ITI-007), has the following structure:

ITI-007 is a potent 5-HT_(2A) receptor ligand (K_(i)=0.5 nM) with a strong affinity for the dopamine (DA) D2 receptor (K_(i)=32 nM) and the serotonin transporter (SERT) (K_(i)=62 nM), but negligible binding to receptors associated with cognitive and metabolic side effects of antipsychotic drugs (e.g., H1 histaminergic, 5-HT_(2C), and muscarinic). ITI-007 is also active at the dopamine D1 receptor (K_(i)=52 nM), and indirectly via this interaction, ITI-007 has been found to result in enhanced NMDA and AMPA signaling in the brain, especially in the medial prefrontal cortex (mPFC). ITI-007 is currently in clinical trials, e.g., for the treatment of schizophrenia, depression, and other psychological disorders. While ITI-007 is a promising drug, its production and formulation present challenges. In free base form, ITI-007 is an oily, sticky solid, with poor aqueous solubility. Making salts of the compound has proven to be unusually difficult. A hydrochloride salt form of ITI-007 was disclosed in U.S. Pat. No. 7,183,282, but this particular salt form was hygroscopic and showed poor stability. It was obtained by precipitation from diethyl ether. A toluenesulfonic acid addition salt (tosylate) of ITI-007 was finally identified and described in WO 2009/114181 and US 2011/0112105 (U.S. Pat. No. 8,648,077).

There is a need for alternative stable and pharmaceutically acceptable salts and polymorphs of ITI-007.

SUMMARY

In an effort to find new salts and polymorphs of ITI-007, an extensive salt screen was undertaken. ITI-007 does not readily form salts with other common, pharmaceutically acceptable acids, despite the good solubility of the free base in a variety of organic solvents. Initially, a toluenesulfonic acid addition salt (tosylate) was prepared, as described in WO 2009/114181 and US 2011/0112105, but no other stable salts were found. Finally, a major salt screen was carried out, wherein the free base compound was studied in different solvent systems and under different conditions, and then systematically screened using a selection of over 100 acids under different conditions and with different solvent, co-solvent and anti-solvent systems, to identify new possible salt forms. Following extensive screening and experimentation, a new bis-tosylate salt polymorph was discovered. This new bistosylate salt form is crystalline and stable.

The present disclosure thus provides a new bis-tosylate salt form of ITI-007, which is especially advantageous for use in the preparation of galenic formulations, together with methods of making and using the same. This disclosure shows that this new bis-tosylate salt form of ITI-007 can be prepared under various conditions, including from the free base form of ITI-007, as well as from the mono-tosylate salt form of ITI-007.

Further areas of applicability of the present invention will become apparent from the detailed description provided hereinafter. It should be understood that the detailed description and specific examples, while indicating preferred embodiments of the invention, are intended for purposes of illustration only and are not intended to limit the scope of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention will become more fully understood from the detailed description and the accompanying drawings.

FIG. 1 depicts overlaid X-ray powder diffraction (XRPD) patterns for the ITI-007 bis-tosylate salt crystal obtained from Example 1 (from a 1:1 molar mixture of ITI-007 free base and toluenesulfonic acid) (upper curve), with reference to the known XRPD pattern for ITI-007 mono-tosylate salt crystal (lower curve).

FIG. 2 depicts the TGA-DSC thermogram of the ITI-007 bis-tosylate salt crystal obtained from Example 1.

FIG. 3 depicts the 1H-NMR spectrum of the ITI-007 bis-tosylate salt crystal obtained from Example 1.

FIG. 4 depicts the FTIR spectrum of the ITI-007 bis-tosylate salt crystal obtained from Example 1.

FIG. 5 depicts overlaid X-ray powder diffraction (XRPD) patterns for the ITI-007 mono-tosylate salt crystal obtained from Example 2 (from a 2:1 molar mixture of ITI-007 free base and toluenesulfonic acid) (upper curve), with reference to the known XRPD pattern for ITI-007 mono-tosylate salt crystal (lower curve).

FIG. 6 depicts the TGA-DSC thermogram of the ITI-007 bis-tosylate salt crystal obtained from Example 2.

FIG. 7 depicts the 1H-NMR spectrum of the ITI-007 bis-tosylate salt crystal obtained from Example 2.

DETAILED DESCRIPTION

The following description of the preferred embodiment(s) is merely exemplary in nature and is in no way intended to limit the invention, its application, or uses.

As used throughout, ranges are used as shorthand for describing each and every value that is within the range. Any value within the range can be selected as the terminus of the range. In addition, all references cited herein are hereby incorporated by referenced in their entireties. In the event of a conflict in a definition in the present disclosure and that of a cited reference, the present disclosure controls.

Unless otherwise specified, all percentages and amounts expressed herein and elsewhere in the specification should be understood to refer to percentages by weight. The amounts given are based on the active weight of the material.

In a first embodiment, the invention provides 1-(4-fluorophenyl)-4-((6bR,10aS)-3-methyl-2,3,6b,9, 10, 10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3 -de]quinoxalin-8-yl)-butan-1-one (ITI-007) in stable bis-tosylate salt form (Salt 1). In additional embodiments, the invention further provides the following:

-   -   1.1. Salt 1, wherein the salt is in solid form.     -   1.2. Salt 1 or 1.1, wherein the salt is in crystalline form,         e.g., dry crystalline form.     -   1.3. Salt 1.2, wherein the salt is in a homogeneous crystal         form, e.g., free or substantially free of other forms of         ITI-007, e.g., free or substantially free, e.g., less than 10         wt. %, preferably less than about 5 wt. %, more preferably less         than about 2 wt. %, still preferably less than about 1 wt. %,         still preferably less than about 0.1%, most preferably less than         about 0.01 wt. %, of any amorphous forms.     -   1.4. Any foregoing form of Salt 1, wherein the salt is in         crystalline form, crystallized from 2-butanone solvent.     -   1.5. Any foregoing form of Salt 1, wherein the salt is a         solvate, e.g., a 2-butanone solvate.     -   1.6. Any foregoing form of Salt 1, wherein the salt is not a         solvate.     -   1.7. Any foregoing form of Salt 1, wherein the salt is a         hydrate.     -   1.8. Any foregoing form of Salt 1, wherein the salt is not a         hydrate.     -   1.9. Any foregoing form of Salt 1, wherein the salt is formed by         combining free ITI-007 free base and toluenesulfonic acid in a         molar ratio from 1:1 to 1:3, e.g., a molar ratio from 1:1 to         1:2.2, or from 1:1 to 1:2, or from 1:1 to 1:1.5, or a molar         ratio of about 1:1, or about 1:1.5, or about 1:2, or about         1:2.2.     -   1.10. Any foregoing form of Salt 1, wherein the salt is formed         from a slurry of ITI-007 free base and toluenesulfonic acid in         2-butanone solvent.     -   1.11. Any foregoing form of Salt 1, wherein a DSC/TGA analysis         of the salt shows one endothermic event at about 184° C., and         one exothermic event at about 258° C., e.g. wherein a DSC/TGA         analysis shows the first endothermic event at about         T_(onset)=178° C., T_(peak)=184° C. and ΔE=−88 J/g, and the         second exothermic event at about T_(onset)=242° C.,         T_(peak)=258° C. and ΔE=122 J/g, for example, wherein the first         endothermic event is a melt and the second exothermic event is a         recrystallization.     -   1.12. Any foregoing form of Salt 1, wherein the salt is in the         form of a crystal having an X-ray powder diffraction pattern         corresponding to the d-spacing and/or angle (2-theta) values of         the following table, for example, wherein the pattern comprises         at least five, or at least six, or at least seven, or at least         eight of said values, e.g., taking into account potential         variations due to sample purity and instrument variation, for         example 2θ shifts due to variation in X-ray wavelength, e.g.,         wherein the X-ray powder diffraction pattern is generated using         an X-ray diffractometer with a copper anode and a nickel filter,         e.g., comprising at least those peaks having a relative         intensity of at least 0.4, at least 0.5, or at least 0.6, or         comprising peaks 1, 2, 6, 7, 8, and 9:

XRPD (Cu anode, Ni filter) for Bis- tosylate Salt Crystal Polymorph 1 # Angle d Value Rel. Intensity 1 6.347 13.9139 1.70% 2 8.389 10.53127 18.20% 3 10.453 8.45646 36.00% 4 13.794 6.41449 6.60% 5 14.26 6.20595 24.30% 6 14.661 6.03727 25.20% 7 14.916 5.93459 25.20% 8 15.397 5.75029 31.10% 9 15.925 5.56057 27.10% 10 16.51 5.36504 18.60% 11 17.106 5.1793 54.00% 12 17.895 4.95287 21.80% 13 18.65 4.75399 14.70% 14 19.198 4.61939 3.10% 15 20.488 4.33151 100.00% 16 20.67 4.29368 75.70% 17 20.857 4.25564 68.10% 18 22.468 3.95398 15.00% 19 22.9 3.88029 11.80% 20 23.973 3.709 24.60% 21 25.114 3.54305 12.80% 22 25.919 3.43479 7.90% 23 27.032 3.29588 10.80% 24 27.416 3.25062 27.80% 25 28.738 3.10393 3.90% 26 29.14 3.06208 3.40% 27 30.128 2.96386 6.10% 28 31.645 2.82511 3.00% 29 33.432 2.67815 1.50% 30 35.412 2.53276 5.30% 31 36.475 2.46136 2.30% 32 39.667 2.27035 3.90% 33 42.624 2.11941 2.50% 34 43.595 2.07446 1.80%

-   -   1.13. Any foregoing form of Salt 1, wherein the salt is in the         form of a crystal having an X-ray powder diffraction pattern         corresponding to FIG. 1 (upper curve), e.g., taking into account         potential variations due to sample purity and instrument         variation, for example 2θ shifts due to variation in X-ray         wavelength, e.g., an X-ray powder diffraction pattern         corresponding to FIG. 1 generated using an X-ray diffractometer         with a copper anode and a nickel filter.     -   1.14. Any foregoing form of Salt 1, wherein the salt is in the         form of a crystal having an X-ray powder diffraction pattern         having at least 5, or at least 6, or at least 7, or at least 8,         peaks having angle (2-theta) values selected from the group         consisting of about 6.35, 8.39, 10.45, 13.79, 14.26, 14.66,         14.92, 15.40, 15.93, 16.51, 17.11, 17.90, 18.65, 19.20, 20.49,         20.67, 20.86, 22.47, 22.90, 23.97, 25.11, 25.92, 27.03, 27.42,         28.74, 29.14, 30.13, 31.65, 33.43, 35.41, 36.48, 39.67, 42.62,         and 43.56, taking into account potential variations due to         sample purity and instrument variation, e.g., wherein the X-ray         powder diffraction pattern is generated using an X-ray         diffractometer with a copper anode and a nickel filter.     -   1.15. Any foregoing form of Salt 1, in the form of a crystal         having an X-ray powder diffraction pattern having at least 5, or         at least 6, or at least 7, or at least 8, peaks having d-spacing         values selected from the group consisting of about 13.91, 10.53,         8.46, 6.42, 6.21, 6.04, 5.93, 5.75, 5.56, 5.37, 5.18, 4.95,         4.75, 4.62, 4.33, 4.29, 4.26, 3.95, 3.88, 3.71, 3.54, 3.44,         3.30, 3.25, 3.10, 3.06, 2.96, 2.83, 2.68, 2.53, 2.46, 2.27,         2.12, and 2.07, taking into account potential variations due to         sample purity and instrument variation, wherein the X-ray powder         diffraction pattern is generated using an X-ray diffractometer         with a copper anode and a nickel filter.     -   1.16. Any foregoing form of Salt 1, wherein the salt is in the         form of a crystal having an X-ray powder diffraction pattern         having at least 5, or at least 6, or at least 7, or at least 8,         peaks having angle (2-theta) values and/or d-spacing values as         provided in Salts 1.14 and/or 1.15.     -   1.17. Any foregoing form of Salt, wherein the salt is in the         form of a crystal having an X-ray powder diffraction pattern         having at least a peak of 25% relative intensity at an angle         (2-theta) value of 10.2-10.5 (e.g., 10.3-10.5, or about 10.3, or         about 10.4 or about 10.45, or about 10.5), optionally, wherein         said peak has a relative intensity of at least 30% or at least         40% or at least 50%, or about 25% or about 30%, or about 35%.     -   1.18. Any foregoing form of Salt 1, wherein the salt is in the         form of a crystal having an X-ray powder diffraction powder         having relative angle (2-theta) values as provided in the table         of embodiment 1.12, wherein the values are shifted by up to         +/−0.2 degrees, e.g., wherein the values are substantially         uniformly shifted by up to +/−0.2 degrees.     -   1.19. Any foregoing form of Salt 1, wherein the salt is in the         form of a crystal having an X-ray diffraction pattern as shown,         or substantially as shown, in the upper curve of FIG. 1.     -   1.20. Any foregoing form of Salt 1, wherein the salt is in the         form of a crystal having a DSC/TGA thermogram as shown, or         substantially as shown, in FIG. 2.     -   1.21. Any foregoing form of Salt 1, wherein the salt has a         proton NMR spectrum as shown, or substantially as shown, in FIG.         3.     -   1.22. Any foregoing form of Salt 1, wherein the salt has a         proton NMR spectrum indicating the presence of about two         toluenesulfonic acid moieties per ITI-007 base moiety, e.g., as         demonstrated by the NMR proton peaks at (i.e., the multiplets         centered at) about 7.11 ppm, 7.36 ppm, 7.49 ppm and 8.03 ppm at         about an integral ratio of 4:2:4:2 (when the spectrum is taken         at 400 MHz in DMSO-d6 solvent).     -   1.23. Any foregoing form of Salt 1, wherein the salt has an FTIR         spectrum as shown, or substantially as shown, in FIG. 4.     -   1.24. Any foregoing form of Salt 1, wherein the salt contains         less than 10 wt % of any other ITI-007 tosylate salt form (e.g.,         mono-tosylate salt or tri-tosylate salt), e.g., less than 5%, or         less than 3%, or less than 2%, or less than 1%, or less than         0.5%, by weight of Salt 1.     -   1.25. Any foregoing form of Salt 1, wherein the salt contains         less than 10 wt % of ITI-007 free base form, e.g., less than 5%,         or less than 3%, or less than 2%, or less than 1%, or less than         0.5%, by weight of Salt 1.     -   1.26. Any foregoing form of Salt 1, wherein the ITI-007 is         deuterated, e.g., wherein the deuterium:protium ratio at one or         more specified positions in the molecule is significantly         higher, e.g., at least 2x, for example at least 10x higher, than         the natural isotope ratios or the isotope ratios at other         positions in the molecule; for example, any foregoing form of         Salt 1 wherein the —CH₂— adjacent to the methylated nitrogen         moiety and/or adjacent to the carbonyl moiety of ITI-007 is         deuterated, e.g., is in the form of —CHD- or —CD₂- at levels         which are significantly higher than the natural         deuterium:protium isotope ratio or the deuterium:protium isotope         ratio at other positions in the molecule, and/or wherein the         methyl group is deuterated, e.g., is CD₃-, e.g., at levels which         are significantly higher than the natural deuterium:protium         isotope ratio or the deuterium:protium isotope ratio at other         positions in the molecule, e.g., as described in WO 2015/154025         (and U.S. Pat. Pub. 2017/0183350) or as described in WO         2017/165843 (equivalent to U.S. application Ser. No.         16/088,397), the contents of each of which are incorporated         herein by reference.     -   1.27. Any foregoing form of Salt 1, wherein the salt exhibits         any combination of characteristics as described in 1.1-1.26.

In another embodiment, the invention provides a process (Process 1) for the production of Salt 1, comprising

-   -   (a) reacting         1-(4-fluorophenyl)-4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxalin-8-yl)-butan-1-one         (ITI-007) free base with toluenesulfonic acid, e.g., together         with an organic solvent (e.g., comprising 2-butanone), for         example, wherein the ITI-007 free base and toluenesulfonic acid         are in a molar ratio from 1:1 to 1:3, e.g., a molar ratio from         1:1 to 1:2.2, or from 1:1 to 1:2, or from 1:1 to 1:1.5, ora         molar ratio of about 1:1, or about 1:1.5, or about 1:2, or about         1:2.2; and     -   (b) recovering the salt thus formed, e.g., recovering Salt 1 or         any of Salts 1.1-1.27.

In another embodiment of Process 1, the reaction step (a) comprises dissolving or suspending the ITI-007 free base in an organic solvent, e.g., 2-butanone, and adding thereto the toluenesulfonic acid. In another embodiment of Process 1, the reaction step (a) comprises combining the ITI-007 free base with the toluenesulfonic acid and adding thereto an organic solvent, e.g., 2-butanone.

In some embodiments of Process 1, the process step (a) is carried out as a batch process, and in other embodiments the process step (a) is carried out as a continuous (flow) process.

In another embodiment, the invention provides a pharmaceutical composition comprising Salt 1, or any of Salts 1.1-1.27, as active ingredient, in combination or association with a pharmaceutically acceptable diluent or carrier.

In another embodiment, the invention provides a pharmaceutical composition comprising Salt 1, or any of Salts 1.1-1.27, as active ingredient, in combination or association with a pharmaceutically acceptable diluent or carrier, wherein the salt is predominantly, or is entirely or substantially entirely, in dry crystalline form.

In a particular embodiment, the invention provides a pharmaceutical composition comprising Salt 1, or any of Salts 1.1-1.27, as active ingredient, in combination or association with a pharmaceutically acceptable diluent or carrier, wherein the composition is in the form of an injectable depot, e.g., to provide extended release of ITI-007.

In another embodiment, the invention provides a pharmaceutical composition (Composition 2) comprising:

-   -   (1) (a)         1-(4-fluorophenyl)-4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3         -de]quinoxalin-8-yl)-butan-1-one (ITI-007) free base or (b) an         acid addition salt of         1-(4-fluorophenyl)-4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3         -de]quinoxalin-8-yl)-butan-1-one (ITI-007) free base, and     -   (2) at least 1 molar equivalent of toluenesulfonic acid based on         the amount of 1-(4-fluorophenyl)-4-((6bR, 10aS)-3         -methyl-2,3,6b, 9,10,         10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3         -de]quinoxalin-8-yl)-butan-1-one (ITI-007) present. Optionally         the acid addition salt of ITI-007 in part (1)(b) is a         hydrochloride salt of ITI-007.

In another embodiment, the invention provides a method of making Composition 2 comprising the steps of:

-   -   (1) Combining either (a)         1-(4-fluorophenyl)-4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3         -de]quinoxalin-8-yl)-butan-1-one (ITI-007) free base     -   or (b) an acid addition salt of         1-(4-fluorophenyl)-4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3         -de]quinoxalin-8-yl)-butan-1-one (ITI-007) free base, with     -   (2) at least 1 molar equivalent of toluenesulfonic acid based on         the amount of         1-(4-fluorophenyl)-4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3         -de]quinoxalin-8-yl)-butan-1-one (ITI-007) present, and     -   (3) mixing the components with at least one pharmaceutically         acceptable diluent or carrier to form the Composition.

In another embodiment, the invention provides Salt 1, or any of Salts 1.1-1.27, or a pharmaceutical composition comprising Salt 1, or any of Salts 1.1-1.27, for use in treating a disease or abnormal condition involving or mediated by the 5-HT_(2A) receptor, serotonin transporter (SERT), and/or dopamine D₁/D₂ receptor signaling pathways, e.g., a disorder selected from obesity, anorexia, bulimia, depression, anxiety, psychosis, schizophrenia, migraine, obsessive-compulsive disorder, sexual disorders, bipolar depression, attention deficit disorder, attention deficit hyperactivity disorder, sleep disorders, conditions associated with cephalic pain, social phobias, and/or dementia.

In another embodiment, the invention provides a method for the prophylaxis or treatment of a human suffering from a disease or abnormal condition involving or mediated by the 5-HT_(2A) receptor, serotonin transporter (SERT), and/or dopamine D₁/D₂ receptor signaling pathways, e.g., a disorder selected from obesity, anorexia, bulimia, depression, anxiety, psychosis, schizophrenia, migraine, obsessive-compulsive disorder, sexual disorders, bipolar depression, attention deficit disorder, attention deficit hyperactivity disorder, sleep disorders, conditions associated with cephalic pain, social phobias, and/or dementia, the method comprising administering to a patient in need thereof a therapeutically effective amount of Salt 1, or any of Salts 1.1-1.27.

EXAMPLE S

The following equipment and methods are used to isolate and characterize the exemplified salt forms:

X-ray powder diffraction (XRPD): The X-ray powder diffraction studies are performed using a Bruker AXS D2 PHASER in Bragg-Brentano configuration, equipment #1549/#2353. The equipment uses a Cu anode at 30 kV, 10 mA; sample stage standard rotating; monochromatization by a Kβ-filter (0.5% Ni). Slits: fixed divergence slits 1.0 mm (=0.61°), primary axial Soller slit 2.5°, secondary axial Soller slit 2.5°. Detector: Linear detector LYNXEYE with receiving slit 5° detector opening. The standard sample holder (0.1 mm cavity in (510) silicon wafer) has a minimal contribution to the background signal. Measurement conditions: scan range 5-45° 2θ, sample rotation 5 rpm, 0.5 s/step, 0.010° /step, 3.0 mm detector slit; and all measuring conditions are logged in the instrument control file. As system suitability, corundum sample A26-B26-S (NIST standard) is measured daily. The software used for data collection is Diffrac.Commander v2.0.26. Data analysis is done using Diffrac.Eva v1.4. No background correction or smoothing is applied to the patterns.

Simultaneous thermogravimetry (TGA) and differential scanning calorimetry (DSC) or TGA/DSC analysis: The TGA/DSC studies are performed using a Mettler Toledo TGA/DSC1 Stare System, equipment #1547, auto-sampler equipped, using pin-holed Al-crucibles of 40 μl. Measurement conditions: 5 min 30.0° C., 30.0-350.0° C. with 10° C./min., N₂ flow of 40 ml/min. The software used for instrument control and data analysis is STARe v12.10.

Differential scanning calorimetry (DSC): The DSC studies are performed using a Mettler Toledo DSC1 STARe System, equipment #1564. The samples are made using Al crucibles (40 μl; pierced). Typically, 1 to 8 mg of sample is loaded onto a pre-weighed Al crucible and is kept at 30° C. for 5 minutes, after which it is heated at 10° C./min from 30° C. to 350° C. and kept at 350° C. for 1 minute. A nitrogen purge of 40 ml/min is maintained over the sample. As system suitability checks, Indium and Zinc are used as references. The software used for data collection and evaluation is STARe Software v12.10 build 5937. No corrections are applied to the thermogram.

Fourier transform infrared spectroscopy (FT-IR): The FT-IR studies are performed using a Thermo Scientific Nicolet iS50, equipment # 2357. An attenuated total reflectance (ATR) technique is used with a beam splitter of KBr. Number of scans is 16 with a resolution of 4, from 400 cm⁻¹ to 4000 cm⁻¹. The software OMNIC version 9.2 is used for data collection and evaluation.

High performance liquid chromatography (HPLC): The high performance liquid chromatography analyses are performed on an LC-31, equipped with an Agilent 1100 series G1322A degasser equipment #1894, an Agilent 1100 series G1311A quaternary pump equipment #1895, an Agilent 1100 series G1313A ALS equipment #1896, an Agilent 1100 series G1318A column equipment #1897 and an Agilent 1100 series G1314A VWD equipment #1898/LC-34, equipped with an Agilent 1200 series G1379B degasser equipment #2254, an Agilent 1100 series G1311A quaternary pump equipment #2255, Agilent 1100 series G1367A WPALS equipment #1656, an Agilent 1100 series G1316A column equipment #2257 and an Agilent 1100 series G1315B DAD equipment #2258. Data is collected and evaluated using Agilent ChemStation for LC systems Rev. B.04.02[96]. Solutions are prepared as follows: Mobile phase A: Add 800 ml of MilliQ water to a 1L volumetric flask. Add 1 ml of TFA and homogenize. Fill up to the mark with MilliQ. Mobile phase B: Add 800 ml of Acetonitrile to a 1L volumetric flask. Add 1 ml of TFA and homogenize. Fill up to the mark with Acetonitrile; Diluent: 50/50 MeOH/ACN.

Proton Nuclear Magnetic Resonance (NMR): Samples are prepared in DMSO-d6 solvent, and spectra are collected on an Agilent Inova400 at room temperature, and at a frequency of 399.9 MHz, with a sweep width of 6398 Hz, and spin of 20 Hz.

Example 1 ITI-007 Bis-Tosylate Salt

Approximately one gram of ITI-007 free base and one molar equivalent of toluenesulfonic acid is combined and mixed with 2-butanone solvent (20 mL). The mixture is stirred at 500 rpm at room temperature for 25 hours. The mixture is then filtered and dried to give a white/brown solid. The solid is analyzed by XRPD, DSC/TGA, HPLC, FTIR and proton NMR. The solid is found to be soluble in methanol and acetic acid (>30 mg/mL), and sparingly soluble in dichloromethane (10-30 mg/mL).

XRPD analysis shows the obtained solid to be a crystalline solid. The XRPD pattern is shown in FIG. 1 (upper curve) with reference to the XRPD pattern obtained from a previously made ITI-007 mono-tosylate salt crystal (lower curve). The reference crystal was obtained from a 1:1 molar mixture of ITI-007 and toluenesulfonic acid using ethyl acetate or toluene as solvent. The results show clear differences in the XPRD pattern between the solid obtained by Example 1 and the reference ITI-007 mono-tosylate salt. One key distinguishing peak that is believed to signal formation of the bis-tosylate salt appears at an angle (2-theta) of about 10.45. The peaks for the compound of Example 1 are identified in tabular form in table 1:

TABLE 1 XRPD peak list for ITI-007 Bis-tosylate Salt of Example 1 # Angle d Value Rel. Intensity 1 6.347 13.9139 1.70% 2 8.389 10.53127 18.20% 3 10.453 8.45646 36.00% 4 13.794 6.41449 6.60% 5 14.26 6.20595 24.30% 6 14.661 6.03727 25.20% 7 14.916 5.93459 25.20% 8 15.397 5.75029 31.10% 9 15.925 5.56057 27.10% 10 16.51 5.36504 18.60% 11 17.106 5.1793 54.00% 12 17.895 4.95287 21.80% 13 18.65 4.75399 14.70% 14 19.198 4.61939 3.10% 15 20.488 4.33151 100.00% 16 20.67 4.29368 75.70% 17 20.857 4.25564 68.10% 18 22.468 3.95398 15.00% 19 22.9 3.88029 11.80% 20 23.973 3.709 24.60% 21 25.114 3.54305 12.80% 22 25.919 3.43479 7.90% 23 27.032 3.29588 10.80% 24 27.416 3.25062 27.80% 25 28.738 3.10393 3.90% 26 29.14 3.06208 3.40% 27 30.128 2.96386 6.10% 28 31.645 2.82511 3.00% 29 33.432 2.67815 1.50% 30 35.412 2.53276 5.30% 31 36.475 2.46136 2.30% 32 39.667 2.27035 3.90% 33 42.624 2.11941 2.50% 34 43.595 2.07446 1.80%

The DSC/TGA thermogram is shown in FIG. 2. DSC/TGA analysis shows one endothermic event at about 184° C., and one exothermic event at about 258° C. The first endothermic event occurs at about T_(onset)=178° C., with a T_(peak)=184° C. and a ΔE=−88 J/g. The second exothermic event occurs at about T_(onset)=242° C., with a T_(peak)=258° C. and a ΔE=122 J/g. The endothermic event is a melt, while the exothermic event is a recrystallization. The TGA profile shows a mass loss of 1.7% from 40° C. to 190° C., and a mass loss of 3.4% from 210° C. to 270° C. It is noted that the recrystallization event occurs at a temperature about 25° C. lower than that previously observed for the reference ITI-007 mono-tosylate salt crystal.

LC-MS analysis shows a purity of 92 area% for the obtained solid.

Proton NMR is shown in FIG. 3. Proton NMR analysis shows that the compound is the bis-tosylate salt of ITI-007. Specifically, the proton NMR spectrum shows the presence of about two toluenesulfonic acid moieties per ITI-007 base moiety. This is demonstrated by the NMR protons at about 7.11 ppm, 7.36 ppm, 7.49 ppm and 8.03 ppm, which are present at an integral ratio of about 4:2:4:2. The 7.11 and 7.49 ppm peaks represent protons from the aromatic tosylate ring of the toluene sulfonate moiety, while the 7.36 and 8.03 peaks represent protons from the aromatic 4-fluorophenyl ring of the ITI-007 moiety. The remaining aromatic peaks between 6.4 and 7.0 ppm represent the aromatic protons of the quinoxaline core of ITI-007 and their integral is consistent with one molar unit of ITI-007 free base. The alkyl peak at about 2.3 ppm represents the methyl group of the tosylate rings and its integral is also consistent with two molar units of toluenesulfonic acid.

The FTIR spectrum is shown in FIG. 4, and it is also consistent with a bis-tosylate structure of the salt.

Dynamic vapor sorption (DVS) analysis shows a stepwise sorption with a total mass uptake at 95 RH % of 2%. This salt is thus slightly hygroscopic. Analysis results are summarized in Table 2 below.

TABLE 2 Analytical results for ITI-007 Bis-tosylate Salt of Example 1 DVS TGA: Hygro- DSC DSC Mass HPLC scopicity (T_(peak) (ΔE loss purity Solvent Appearance (%) ° C.) J/g) (%) (area %) 2- White/brown 2 184  −88 1.7 92 Butanone solid 258 +121 3.4

In direct comparison to the analytical data obtained on the mono-tosylate salt of Example 2, it is apparent that the salt of Example 1 is a distinct crystalline salt form comprising a 1:2 molar ratio of ITI-007 free base to toluene sulfonic acid. Without being bound by theory, it is believed that the lower solubility of ITI-007 free base in 2-butanone solvent, compared to other solvents, result in the effective concentration of free base being lower, and the effective ratio of free base to toluenesulfonic acid being higher. As a result, the bis-tosylate salt forms and unreacted free base remains in solution after filtration of the product.

Additional experiments demonstrate that at a 1:2 molar ratio of ITI-007 free base to toluenesulfonic acid in 2-butanone solvent, conducted substantially as described above, the solid collected after filtration is the same bis-tosylate salt as described above in high to quantitative yield.

Example 2 ITI-007 Mono-Tosylate Salt

Approximately one gram of ITI-007 free base and one-half molar equivalent of toluenesulfonic acid is added mixed with 2-butanone solvent (15 mL). The mixture is stirred at 500 rpm at room temperature for 25 hours. The mixture is then filtered and dried to give a white solid. The solid is analyzed by XRPD, DSC/TGA, HPLC, FTIR and proton NMR. The analysis demonstrates that this salt is a mono-tosylate salt of ITI-007 and it is distinctly different from the bis-tosylate salt obtained from Example 1.

XRPD analysis shows the obtained solid to be a crystalline solid. The XRPD pattern is shown in FIG. 5 (upper curve) with reference to the XRPD pattern obtained from a previously made ITI-007 mono-tosylate salt crystal (lower curve). The reference crystal was obtained from a 1:1 molar mixture of ITI-007 and toluenesulfonic acid using ethyl acetate or toluene as solvent. The results show substantially the same XPRD pattern between the solid obtained by Example 2 and the reference ITI-007 mono-tosylate salt. The peaks for the compound of Example 2 are identified in tabular form in table 3:

TABLE 3 XRPD peak list for ITI-007 Mono-tosylate Salt of Example 2 # Angle d Value Rel. Intensity 1 8.463 10.43945 9.70% 2 11.331 7.80275 15.20% 3 12.059 7.33324 47.30% 4 13.285 6.65902 23.70% 5 14.142 6.25762 1.00% 6 14.987 5.90646 3.20% 7 15.802 5.6038 21.50% 8 15.929 5.55918 18.40% 9 16.381 5.40706 13.20% 10 16.993 5.21366 100.00% 11 17.432 5.08331 7.80% 12 18.096 4.89827 18.90% 13 18.938 4.68221 16.60% 14 19.218 4.61464 6.30% 15 19.854 4.46835 29.10% 16 20.686 4.29037 4.00% 17 21.612 4.10869 9.40% 18 22.557 3.93865 35.70% 19 22.757 3.90439 26.00% 20 23.442 3.79192 24.90% 21 23.642 3.7602 11.20% 22 24.263 3.66543 39.40% 23 25.727 3.46008 6.50% 24 25.912 3.43574 7.40% 25 27.162 3.28038 4.30% 26 29.604 3.01515 3.30% 27 30.804 2.90033 1.60% 28 31.551 2.83332 3.10% 29 32.265 2.77228 2.30% 30 34.662 2.58583 3.60% 31 36.82 2.43906 1.60% 32 37.497 2.39657 1.60% 33 39.386 2.28588 1.30%

The DSC/TGA thermogram is shown in FIG. 6. DSC/TGA analysis shows one endothermic event at about 179° C., and one exothermic event at about 285° C. The first endothermic event occurs at about T_(onset)=175° C., with a T_(peak)=179° C. and a ΔE=−81 J/g. The second exothermic event occurs at about T_(onset)=278° C., with a T_(peak)=285° C. and a ΔE=255 J/g. The endothermic event is a melt, while the exothermic event is a recrystallization. The TGA profile shows a mass loss of 0.4% from 40° C. to 220° C., and a mass loss of 9.4% from 220° C. to 290° C.

LC-MS analysis shows a purity of 93 area % for the obtained solid.

Proton NMR is shown in FIG. 7. Proton NMR analysis shows that the compound is the mono-tosylate salt of ITI-007. Specifically, the spectrum proton NMR spectrum shows the presence of one toluenesulfonic acid moiety per ITI-007 base moiety. This is demonstrated by the NMR protons at about 7.11 ppm, 7.36 ppm, 7.52 ppm and 8.05 ppm, which are present at an integral ratio of about 2:2:2:2. The 7.11 and 7.52 ppm peaks represent protons from the aromatic tosylate ring, while the 7.36 and 8.05 peaks represent protons from the aromatic 4-fluorophenyl ring of the ITI-007 free base. The remaining aromatic peaks between 6.4 and 7.0 ppm represent the aromatic protons of the quinoxaline core of ITI-007 and their integral is consistent with one molar unit of ITI-007 free base (integrals in a 1:1:1 ratio of clearly distinct peaks). The alkyl peak at about 2.3 ppm represents the methyl group of the tosylate ring and its integral is also consistent with one molar unit of toluenesulfonic acid.

Analytical results are summarized in Table 4 below.

TABLE 4 Analytical results for ITI-007 Mono-tosylate Salt of Example 2 Appear- DSC DSC TGA: Mass HPLC purity Solvent ance (T_(peak)° C.) (ΔE J/g) loss (%) (area %) 2-Butanone White 179 −81 0.4 93 solid 285 +255 9.4 

1. A stable bis-tosylate salt of 1-(4-fluorophenyl)-4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4, 5]pyrrolo[1,2,3-de]quinoxalin-8-yl)-butan-1-one, e.g., in a homogenous crystal form, free or substantially free of other forms of 1-(4-fluorophenyl)-4-((6bR, 10aS)-3 -methyl-2,3 ,6b,9, 10, 10a-hexahy dro-1H,7H-pyrido[3′,4′:4,5]pyrrol 0[1,2,3 -de]quinoxalin-8-yl)-butan-1-one.
 2. The salt according to claim 1, which is a salt formed by combining free ITI-007 free base and toluenesulfonic acid in a molar ratio from 1:1 to 1:3.
 3. The salt according to claim 1, wherein the salt is formed from a slurry of ITI-007 free base and toluenesulfonic acid in 2-butanone solvent.
 4. The salt according to claim 1, which is a salt crystal having an X-ray diffraction pattern as shown, or substantially as shown, in the upper curve of FIG.
 1. 5. The salt according to claim 1, which is a salt crystal having a DSC/TGA thermogram as shown, or substantially as shown, in FIG.
 2. 6. The salt according to claim 1, which is a salt crystal having a proton NMR spectrum as shown, or substantially as shown, in FIG.
 3. 7. The salt according to claim 1, which is a salt crystal having a proton NMR spectrum indicating the presence of about two toluenesulfonic acid moieties per ITI-007 base moiety.
 8. The salt according to claim 1, wherein the salt contains less than 10 wt % of any other ITI-007 tosylate salt form.
 9. The salt according to claim 1, wherein the salt contains less than 10 wt % of ITI-007 free base form.
 10. A method making a salt according to claim 1, comprising (a) reacting 1-(4-fluoro-phenyl)-4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxalin-8-yl)-butan-1-one (ITI-007) free base with toluenesulfonic acid. and (b) recovering the salt thus formed.
 11. The method according to claim 10, wherein the reaction is carried out in an organic solvent.
 12. A pharmaceutical composition comprising the salt according to claim 1, in combination or association with a pharmaceutically acceptable diluent or carrier.
 13. A method for the prophylaxis or treatment of a human suffering from a disease or abnormal condition involving or mediated by the 5-HT_(2A) receptor, serotonin transporter (SERT), and/or dopamine D₁/D₂ receptor signaling pathways comprising administering to said human an effective amount of a salt according to claim
 1. 